54422 Results for: "D-Proline+methyl+ester+hydrochloride"

Supplier: Bioss

Glutamate receptors mediate most excitatory neurotransmission in the brain and play an important role in neural plasticity, neural development and neurodegeneration. Ionotropic glutamate receptors are categorized into NMDA receptors and kainate/AMPA receptors, both of which contain glutamate-gated, cation-specific ion channels. Synaptic and extrasynaptic NMDA receptors have been shown to have opposite effects on neuronal survival, CREB function and gene regulation. As one of the four major proteins of the NMDA receptor ion channel, GRINA (Glutamate [NMDA] receptor-associated protein 1), also designated NMDA receptor glutamate-binding subunit or putative MAPK-activating protein PM02, is a 371 amino acid multi-pass transmembrane protein. Due to the chromosomal location of the gene encoding GRINA, studies have linked possible GRINA involvement with a form of idiopathic generalized epilepsy.

Supplier: Bioss

Glutamate receptors mediate most excitatory neurotransmission in the brain and play an important role in neural plasticity, neural development and neurodegeneration. Ionotropic glutamate receptors are categorized into NMDA receptors and kainate/AMPA receptors, both of which contain glutamate-gated, cation-specific ion channels. Synaptic and extrasynaptic NMDA receptors have been shown to have opposite effects on neuronal survival, CREB function and gene regulation. As one of the four major proteins of the NMDA receptor ion channel, GRINA (Glutamate [NMDA] receptor-associated protein 1), also designated NMDA receptor glutamate-binding subunit or putative MAPK-activating protein PM02, is a 371 amino acid multi-pass transmembrane protein. Due to the chromosomal location of the gene encoding GRINA, studies have linked possible GRINA involvement with a form of idiopathic generalized epilepsy.

Supplier: TriLink BioTechnologies

TriLink's patented CleanCap® Reagent M6 [CleanCap m6AG (3′ OMe)], is designed for the co-transcriptional capping of mRNA to produce an mRNA with base-modified Cap 1. Cap-1 mRNAs have superior in vivo activity compared to Cap-0 mRNAs produced by legacy capping methods.

Supplier: Bioss

Glutamate receptors mediate most excitatory neurotransmission in the brain and play an important role in neural plasticity, neural development and neurodegeneration. Ionotropic glutamate receptors are categorized into NMDA receptors and kainate/AMPA receptors, both of which contain glutamate-gated, cation-specific ion channels. Synaptic and extrasynaptic NMDA receptors have been shown to have opposite effects on neuronal survival, CREB function and gene regulation. As one of the four major proteins of the NMDA receptor ion channel, GRINA (Glutamate [NMDA] receptor-associated protein 1), also designated NMDA receptor glutamate-binding subunit or putative MAPK-activating protein PM02, is a 371 amino acid multi-pass transmembrane protein. Due to the chromosomal location of the gene encoding GRINA, studies have linked possible GRINA involvement with a form of idiopathic generalized epilepsy.

Supplier: MP Biomedicals

Purity: 98% 1 * 1 g

Supplier: MP Biomedicals

Purity: 98% 1 * 25 g

Supplier: MP Biomedicals

Anti-bacterial Agent 1 * 25 g

Supplier: MP Biomedicals

Anti-bacterial Agent 1 * 50 g

Supplier: MP Biomedicals

Purity: 98% 1 * 5 g

Supplier: MP Biomedicals

Anti-bacterial Agent 1 * 5 g

Supplier: Cayman Chemical

Rauwolscine is a natural alkaloid that acts as a selective and reversible 2-adregenergic receptor antagonist (Ki = 12 nM).{25653} I t is a stereoisomer of yohimbine, which potently antagonizes both 1- and 2-adrenergic receptors.{25653} Rauwolscine 1 * 250 mg

Supplier: Cayman Chemical

Atipamezole is an imidazole that potently antagonizes the 2-adrenoceptor (Ki = 1.6 nM).{25705,25706} It shows selectivity over the 1-adrenoceptor (Ki = 13,300 nM) and is a poor antagonist at a wide variety of other receptors and channels.{25706} Th 1 * 5 mg

Supplier: G-Biosciences

Tetracycline is a bacteriostatic antibiotic with activity against both gram-positive and gram-negative bacteria. Within the cell tet racycline binds reversibly to the 30S subunit of the ribosome, preventing the binding of aminoacyl tRNA and inhibitin 1 * 25 g

Supplier: Cayman Chemical

Rauwolscine is a natural alkaloid that acts as a selective and reversible 2-adregenergic receptor antagonist (Ki = 12 nM).{25653} I t is a stereoisomer of yohimbine, which potently antagonizes both 1- and 2-adrenergic receptors.{25653} Rauwolscine 1 * 100 mg

Supplier: MP Biomedicals

UN2811III 1 * 50 mg

Supplier: Cayman Chemical

Atipamezole is an imidazole that potently antagonizes the 2-adrenoceptor (Ki = 1.6 nM).{25705,25706} It shows selectivity over the 1-adrenoceptor (Ki = 13,300 nM) and is a poor antagonist at a wide variety of other receptors and channels.{25706} Th 1 * 50 mg

Supplier: LGC Standards PROMOCHEM

(2S,3S)-2-(4-Methoxyphenyl)-4-oxo-2,3,4,5- tetrahydro-1,5-benzothiazepin-3-yl Acetate 1 * 25 mg

Supplier: LGC Standards PROMOCHEM

(2S,3S)-5-[2-(Dimethylamino)ethyl]-3- hydroxy-2-(4-methoxyphenyl)-2,3- dihydro-1,5-benzothiazepin-4(5H)-one 1 * 25 mg

Supplier: LGC Standards PROMOCHEM

(2S,3S)-2-(4-Methoxyphenyl)-5-[2-(methylamino)ethyl]-4-oxo-2,3,4 ,5-tetrahydro-1,5-benzothiazepin-3-yl Acetate 1 * 25 mg

Supplier: LGC Standards PROMOCHEM

(2S,3S)-3-Hydroxy-2-(4- methoxyphenyl)-2,3-dihydro-1,5- benzothiazepin-4(5H)-one 1 * 25 mg

Supplier: Cayman Chemical

Rauwolscine is a natural alkaloid that acts as a selective and reversible 2-adregenergic receptor antagonist (Ki = 12 nM).{25653} I t is a stereoisomer of yohimbine, which potently antagonizes both 1- and 2-adrenergic receptors.{25653} Rauwolscine 1 * 50 mg

Supplier: Cayman Chemical

Atipamezole is an imidazole that potently antagonizes the 2-adrenoceptor (Ki = 1.6 nM).{25705,25706} It shows selectivity over the 1-adrenoceptor (Ki = 13,300 nM) and is a poor antagonist at a wide variety of other receptors and channels.{25706} Th 1 * 25 mg

Supplier: Cayman Chemical

Atipamezole is an imidazole that potently antagonizes the 2-adrenoceptor (Ki = 1.6 nM).{25705,25706} It shows selectivity over the 1-adrenoceptor (Ki = 13,300 nM) and is a poor antagonist at a wide variety of other receptors and channels.{25706} Th 1 * 10 mg

Supplier: Merck Millipore (Calbiochem‎)

Whi-P180 1 * 1 mg

Supplier: STEMCELL Technologies

Cl-Amidine 1 * 1 mg

Supplier: SI Analytics

Cleaning solution L5104, DURAN® bottle, cleaning solution pepsin/hydrochloric acid 1 * 250 mL

Supplier: SI Analytics

Cleaning solution L 510 pepsin/hydrochloric acid 1 * 1 L

Supplier: LGC Standards PROMOCHEM

2-(BENZYLMETHYLAMINO)-1-(3-HYDROXYPHENYL 1 * 100 mg

Supplier: Merck Millipore (Calbiochem‎)

Bisindolylmaleimide I Hcl 1 * 1 mg

Supplier: Merck Millipore (Calbiochem‎)

W-13 Hcl 1 * 1 mg